FDA 510(k) Applications Submitted by INBIOS INTERNATIONAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K181473 06/04/2018 DENV Detect NS1 ELISA InBios International, Inc.
DEN220044 07/08/2022 Active Anthrax DetectTM Plus Rapid Test InBios International, Inc.
K161947 07/14/2016 Chagas Detect Plus Rapid Test INBIOS INTERNATIONAL, INC.
DEN180069 12/26/2018 ZIKV Detect 2.0 IgM Capture ELISA InBios International, Inc.


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